Literature DB >> 24333264

Antioxidant gene therapy against neuronal cell death.

Juliana Navarro-Yepes1, Laura Zavala-Flores2, Annadurai Anandhan2, Fang Wang3, Maciej Skotak3, Namas Chandra3, Ming Li4, Aglaia Pappa5, Daniel Martinez-Fong6, Luz Maria Del Razo7, Betzabet Quintanilla-Vega7, Rodrigo Franco8.   

Abstract

Oxidative stress is a common hallmark of neuronal cell death associated with neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, as well as brain stroke/ischemia and traumatic brain injury. Increased accumulation of reactive species of both oxygen (ROS) and nitrogen (RNS) has been implicated in mitochondrial dysfunction, energy impairment, alterations in metal homeostasis and accumulation of aggregated proteins observed in neurodegenerative disorders, which lead to the activation/modulation of cell death mechanisms that include apoptotic, necrotic and autophagic pathways. Thus, the design of novel antioxidant strategies to selectively target oxidative stress and redox imbalance might represent important therapeutic approaches against neurological disorders. This work reviews the evidence demonstrating the ability of genetically encoded antioxidant systems to selectively counteract neuronal cell loss in neurodegenerative diseases and ischemic brain damage. Because gene therapy approaches to treat inherited and acquired disorders offer many unique advantages over conventional therapeutic approaches, we discussed basic research/clinical evidence and the potential of virus-mediated gene delivery techniques for antioxidant gene therapy.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Antioxidant gene therapy; Brain ischemia; Neurodegenerative disorders; Oxidative stress; ROS; Virus-mediated gene delivery

Mesh:

Substances:

Year:  2013        PMID: 24333264      PMCID: PMC3959583          DOI: 10.1016/j.pharmthera.2013.12.007

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


  437 in total

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